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New poly(diphenylacetylene) compound, preparation method therefor, and use thereof as optical isomer separating agent

a technology of diphenylacetylene and compound, which is applied in the field of new diphenylacetylene compound, preparation method therefor, can solve the problems of inability to analyze general separation methods, and achieve the effects of reducing the number of optical isomers, avoiding chromaticity, and avoiding chromaticity

Inactive Publication Date: 2015-12-31
KANAZAWA UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The present invention concerns an optically active compound (I) that has superior optical resolution ability for a wide variety of compounds and is not easily racemized at room temperature. This compound has a unique helical structure that allows for various chemical modification after induction and memory of helical chirality. Compared to conventional optical isomer separating agents, this compound is advantageous in cost and can produce a chiral stationary phase with as high optical resolution ability as using an optically pure compound. Additionally, even a compound with low optical purity can still control the winding direction of helix with the same level of optical purity.

Problems solved by technology

As described above, since optical isomers show completely the same physical and chemical properties, they cannot be analyzed by general separation means.

Method used

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  • New poly(diphenylacetylene) compound, preparation method therefor, and use thereof as optical isomer separating agent
  • New poly(diphenylacetylene) compound, preparation method therefor, and use thereof as optical isomer separating agent
  • New poly(diphenylacetylene) compound, preparation method therefor, and use thereof as optical isomer separating agent

Examples

Experimental program
Comparison scheme
Effect test

example 1

Synthesis of Compound (IIa)

(1) Synthesis of heptyl 4-iodobenzoate (2a)

[0200]

[0201]Under a nitrogen atmosphere, 4-iodobenzoic acid (1a) (10.6 g, 42.9 mmol) was dissolved in anhydrous dichloromethane (140 mL), and several drops of anhydrous N,N-dimethylformamide were added. Thereafter, oxalyl chloride (4.50 mL, 42.4 mmol) was added at 0° C., and the mixture was stirred at room temperature for 10 hr. The solvent was removed, anhydrous pyridine (70 mL) and n-heptanol (7.0 mL, 49.4 mmol) were added, and the mixture was stirred at 70° C. for 5 hr. The reaction solvent was removed, the residue was diluted with ethyl acetate, washed with distilled water and saturated aqueous sodium hydrogen carbonate solution, and the organic layer was dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure, and the residue was purified by column chromatography (ethyl acetate:hexane=1:19) to give heptyl 4-iodobenzoate (2a) (14.5 g, yield 97%) as an oily liquid.

(2) Synthesis of h...

example 2

Induction and Memory of One-Handed Helical Chirality in Optical Inactive Compound (IIa)

[0223]

(1) Induction of Helical Chirality in Compound (IIa)

[0224]Compound (IIa) (200 mg, 0.751 mmol) was dissolved in water (75 mL), and optically pure (S)-(+)-2-phenylglycinol (823 mg, 6.00 mmol) was added. After stirring at 95° C. for 2 hr, the mixture was left standing at 25° C. for 24 hr, and the CD spectrum of the solution was measured (cell length: 0.1 cm, measurement temperature: 25° C.) (FIG. 1(a)). As a result, a clear Cotton effect was observed in the absorption region of the main chain, whereby it was suggested that a one-handed helical structure was induced in compound (IIa), and an optically active compound (Ia) was produced.

(2) Memory of Helical Chirality in Compound (Ia)

[0225]To an aqueous solution of the optically active compound (Ia), in which the one-handed helical structure was induced by the aforementioned treatment, was added sodium hydroxide (33 mg, 0.83 mmol). The mixture wa...

example 3

Synthesis of Optically Active Compound (Ib) by Amidation Reaction of Side Chain Carboxy Group of Optically Active Compound (Ia) Having One-Handed Helical Structure

[0226]

[0227]The optically active compound (Ia) (170 mg, 0.638 mmol) was dissolved in dimethyl sulfoxide / water (5:1, v / v) (30 mL), aniline (238 mg, 2.55 mmol) and 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride (DMT-MM) (706 mg, 2.55 mmol) were added, and the mixture was stirred at room temperature for 5 hr. The precipitated solid was collected by centrifugation, dissolved in a small amount of tetrahydrofuran, reprecipitated in a large amount of a mixed solvent of water / methanol (5:1, v / v), collected by centrifugation, and washed with methanol to give compound (Ib) (186 mg, yield 70%) as a dark red solid. The obtained compound (Ib) was dissolved in dimethyl sulfoxide, and CD was measured. As a result, induced CD similar to that with compound (Ia) having an one-handed helical structure (FIG. 1(c)). Therefo...

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Abstract

The present invention provides an optical isomer separating agent and a production method thereof. That is, the present invention provides a one-handed helical poly(diphenylacetylene) compound represented by the following formula (I)[wherein each symbol is as described in the DESCRIPTION], and a production method thereof, an optical isomer separating agent containing the poly(diphenylacetylene) compound, and a packing material for a chiral column, containing the optical isomer separating agent coated on a carrier. Since these have a superior separation ability for a wide variety of compounds, a practical optical resolution method can be provided.

Description

TECHNICAL FIELD[0001]The present invention relates to an optical isomer separating agent used for separating an optical isomer by a chromatography method, particularly liquid chromatography, and a packing material supporting same, and particularly relates to a helical poly(diphenylacetylene) compound useful as a separating agent for a mixture of optical isomers of a wide variety of chiral compounds and a production method thereof.BACKGROUND ART[0002]Organic compounds include many optical isomers having completely the same physical, chemical properties, for example, properties such as boiling point, melting point, solubility but showing different physiological activities. In the technical field of medicaments, differences in the pharmacological activity depending on the easiness of binding with a particular receptor in the body have been studied much, and it is widely known that remarkable differences in drug, efficacy and toxicity are often found between optical isomers. Guideline f...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): C08F138/02
CPCB01D15/3833C08F38/00B01J20/261B01J20/103C08F138/02B01J20/29B01J20/3204B01J20/327B01J20/328
Inventor MAEDA, KATSUHIROKANOH, SHIGEYOSHIIKAI, TOMOYUKISHIMOMURA, KOUHEIKOMATSU, YUKI
Owner KANAZAWA UNIV
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